Medical Device Recalls
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101 to 104 of 104 Results
510(K) Number: K142297 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| EndoVive 3s Low Profile Balloon Kits Part Number: M00548810 (XMD P/N 70-0050-G18) The EndoVive 3... | 2 | 02/26/2016 | Xeridiem Mediem Medical Devices Inc |
| EndoVive 3s Low Profile Balloon Kits Part Number: M00548970 (XMD P/N 70-0050-G20) The EndoVive 3... | 2 | 02/26/2016 | Xeridiem Mediem Medical Devices Inc |
| EndoVive 3s Low Profile Balloon Kits Part Number: M00549460 (XMD P/N 70-0050-G22) The EndoVive 3... | 2 | 02/26/2016 | Xeridiem Mediem Medical Devices Inc |
| EndoVive 3s Low Profile Balloon Kits Part Number: M00549600 (XMD P/N 70-0050-G24) The EndoVive 3... | 2 | 02/26/2016 | Xeridiem Mediem Medical Devices Inc |
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